2-Fluoro-3-nitrobenzenesulfonyl chloride

Base Information

Chemical Name:2-Fluoro-3-nitrobenzenesulfonyl chloride
CAS No.:86156-97-0
Molecular Formula:C₆H₃ClFNO₄S
Molecular Weight:239.612
Hs Code.:2904990090
European Community (EC) Number:895-518-4

Synonyms:86156-97-0;2-fluoro-3-nitrobenzenesulfonyl chloride;2-Fluoro-3-nitrobenzene-1-sulfonyl chloride;2-FLUORO-3-NITROPHENYLSULFONYL CHLORIDE;SCHEMBL22659312;CL9697;AKOS006239079;2-Fluoro-3-nitrobenzenesulphonyl chloride;2-Fluoro-3-nitrobenzene-1-sulfonylchloride

Suppliers and Price of 2-Fluoro-3-nitrobenzenesulfonyl chloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Crysdot
2-Fluoro-3-nitrobenzene-1-sulfonylchloride 97%
1g
$ 1151.00

Total 5 raw suppliers

Chemical Property of 2-Fluoro-3-nitrobenzenesulfonyl chloride

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:238.9455346
Heavy Atom Count:14
Complexity:322

Purity/Quality:: 2-Fluoro-3-nitrobenzene-1-sulfonylchloride 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=C(C(=C1)S(=O)(=O)Cl)F)[N+](=O)[O-]

Technology Process of 2-Fluoro-3-nitrobenzenesulfonyl chloride

There total 2 articles about 2-Fluoro-3-nitrobenzenesulfonyl chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 573-55-7
2-fluoro-1,3-dinitrobenzene

: 86156-97-0
2-fluoro-3-nitrobenzenesulfonyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 39.1 percent / iron powder / acetic acid / 1.5 h / Heating

2: 1.) 36percent hydrochloric acid, NaNO₂; 2.) CuCl₂, SO₂ / 1.) water, 0 deg C, 30 min; 2.) water, glacial acetic acid, r.t., 30 min

With hydrogenchloride; sulfur dioxide; iron; copper dichloride; sodium nitrite; In acetic acid;
DOI:10.1002/hlca.19830660108

Reference yield:

: 21397-11-5
aminofluoronitrobenzene

: 86156-97-0
2-fluoro-3-nitrobenzenesulfonyl chloride

Guidance literature:: With hydrogenchloride; sulfur dioxide; copper dichloride; sodium nitrite; Yield given. Multistep reaction; 1.) water, 0 deg C, 30 min; 2.) water, glacial acetic acid, r.t., 30 min;
DOI:10.1002/hlca.19830660108

Reference yield:

: 86156-97-0
2-fluoro-3-nitrobenzenesulfonyl chloride

: 2-fluoro-3-nitrobenzenesulfonic acid potassium salt

Guidance literature:: With hydrogenchloride; ethanol; water; potassium carbonate; Yield given. Multistep reaction; 1.) 50 deg C, 30 min; 2.) water, 0 deg C;
DOI:10.1002/hlca.19830660108